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Results: 1-8 |
Results: 8
Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C
Authors: Meiner, V Shpitzen, S Mandel, H Klar, A Ben-Neriah, Z Zlotogora, J Sagi, M Lossos, A Bargal, R Sury, V Carmi, R Leitersdorf, E Zeigler, M
Citation: V. Meiner et al., Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C, GENET MED, 3(5), 2001, pp. 343-348
Multifocal demyelinative leukoencephalopathy associated with 5-fluorouracil and levamisole
Authors: Israel, ZH Lossos, A Barak, V Soffer, D Siegal, T
Citation: Zh. Israel et al., Multifocal demyelinative leukoencephalopathy associated with 5-fluorouracil and levamisole, ACTA ONCOL, 39(1), 2000, pp. 117-120
In vivo assessment of the window of barrier opening after osmotic blood-brain barrier disruption in humans
Authors: Siegal, T Rubinstein, R Bokstein, F Schwartz, A Lossos, A Shalom, E Chisin, R Gomori, JM
Citation: T. Siegal et al., In vivo assessment of the window of barrier opening after osmotic blood-brain barrier disruption in humans, J NEUROSURG, 92(4), 2000, pp. 599-605
Pharmacokinetics of methotrexate in cerebrospinal fluid and serum after osmotic blood-brain barrier disruption in patients with brain lymphoma
Authors: Zylber-Katz, E Gomori, JM Schwartz, A Lossos, A Bokstein, F Siegel, T
Citation: E. Zylber-katz et al., Pharmacokinetics of methotrexate in cerebrospinal fluid and serum after osmotic blood-brain barrier disruption in patients with brain lymphoma, CLIN PHARM, 67(6), 2000, pp. 631-641
Cerebrospinal fluid lactate dehydrogenase isoenzyme analysis for the diagnosis of central nervous system involvement in hematooncologic patients
Authors: Lossos, IS Breuer, R Intrator, O Lossos, A
Citation: Is. Lossos et al., Cerebrospinal fluid lactate dehydrogenase isoenzyme analysis for the diagnosis of central nervous system involvement in hematooncologic patients, CANCER, 88(7), 2000, pp. 1599-1604
Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxia
Authors: Hassin-Baer, S Bar-Shira, A Gilad, S Galanty, Y Khosravi, R Lossos, A Giladi, N Weitz, R Ben-Zeev, B Goldhammer, Y Shiloh, Y
Citation: S. Hassin-baer et al., Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxia, J NEUROL, 246(8), 1999, pp. 716-719
Interferon in the treatment of base of the skull hemangioendothelioma
Authors: Freeman, AI Lossos, A Gomori, JM Schwartz, A Elidan, J Siegal, T
Citation: Ai. Freeman et al., Interferon in the treatment of base of the skull hemangioendothelioma, OTO H N SUR, 121(6), 1999, pp. 842-843
Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr(329)Ser mutation in the glycogen-branching enzyme gene
Authors: Lossos, A Meiner, Z Barash, V Soffer, D Schlesinger, I Abramsky, O Argov, Z Shpitzen, S Meiner, V
Citation: A. Lossos et al., Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr(329)Ser mutation in the glycogen-branching enzyme gene, ANN NEUROL, 44(6), 1998, pp. 867-872
Risultati: 1-8 |